Abstract:We investigated the effects of iron (Fe) and copper (Cu) limitations on biogenic silica (bSiO2) dissolution kinetics of the marine diatom Pseudo‐nitzschia delicatissima during a 3 week batch dissolution experiment. The dissolution of this species was faster during the first week than thereafter. Modeling results from four dissolution models and scanning electron microcopy images suggested the successive dissolution of two phases of bSiO2, with two different dissolution constants. Micronutrient limitation durin… Show more
“…Iron (Fe) availability affects the growth rate, Si uptake, cell morphology and BSi content in diatoms (Leynaert et al, 2004;Hoffmann et al, 2008;Marchetti and Cassar, 2009;Boutorh et al, 2016;Meyerink et al, 2017). These microscale effects can have far reaching consequences on the physico-chemical environment, particularly in the Southern Ocean.…”
The fractionation of silicon (Si) isotopes was measured in two Southern Ocean diatoms (Proboscia inermis and Eucampia Antarctica) and a coastal diatom (Thalassiosira pseudonana) that were grown under varying iron (Fe) concentrations. Varying Fe concentrations had no effect on the Si isotope enrichment factor (ε) in T. pseudonana, whilst E. Antarctica and P. inermis exhibited significant variations in the value of ε between Fe-replete and Fe-limited conditions. Mean ε values in P. inermis and E. Antarctica decreased from (± 1SD) −1.11 ± 0.15‰ and −1.42 ± 0.41 ‰ (respectively) under Fe-replete conditions, to −1.38 ± 0.27 ‰ and −1.57 ± 0.5 ‰ (respectively) under Fe-limiting conditions. These variations likely arise from adaptations in diatoms arising from the nutrient status of their environment. T. pseudonana is a coastal clone typically accustomed to low Si but high Fe conditions whereas E. Antarctica and P. inermis are typically accustomed to High Si, High nitrate low Fe conditions. Growth induced variations in silicic acid (Si(OH) 4) uptake arising from Fe-limitation is the likely mechanism leading to Si-isotope variability in E. Antarctica and P. inermis. The multiplicative effects of species diversity and resource limitation (e.g., Fe) on Si-isotope fractionation in diatoms can potentially alter the Si-isotope composition of diatom opal in diatamaceous sediments and sea surface Si(OH) 4. This work highlights the need for further in vitro studies into intracellular mechanisms involved in Si(OH) 4 uptake, and the associated pathways for Si-isotope fractionation in diatoms.
“…Iron (Fe) availability affects the growth rate, Si uptake, cell morphology and BSi content in diatoms (Leynaert et al, 2004;Hoffmann et al, 2008;Marchetti and Cassar, 2009;Boutorh et al, 2016;Meyerink et al, 2017). These microscale effects can have far reaching consequences on the physico-chemical environment, particularly in the Southern Ocean.…”
The fractionation of silicon (Si) isotopes was measured in two Southern Ocean diatoms (Proboscia inermis and Eucampia Antarctica) and a coastal diatom (Thalassiosira pseudonana) that were grown under varying iron (Fe) concentrations. Varying Fe concentrations had no effect on the Si isotope enrichment factor (ε) in T. pseudonana, whilst E. Antarctica and P. inermis exhibited significant variations in the value of ε between Fe-replete and Fe-limited conditions. Mean ε values in P. inermis and E. Antarctica decreased from (± 1SD) −1.11 ± 0.15‰ and −1.42 ± 0.41 ‰ (respectively) under Fe-replete conditions, to −1.38 ± 0.27 ‰ and −1.57 ± 0.5 ‰ (respectively) under Fe-limiting conditions. These variations likely arise from adaptations in diatoms arising from the nutrient status of their environment. T. pseudonana is a coastal clone typically accustomed to low Si but high Fe conditions whereas E. Antarctica and P. inermis are typically accustomed to High Si, High nitrate low Fe conditions. Growth induced variations in silicic acid (Si(OH) 4) uptake arising from Fe-limitation is the likely mechanism leading to Si-isotope variability in E. Antarctica and P. inermis. The multiplicative effects of species diversity and resource limitation (e.g., Fe) on Si-isotope fractionation in diatoms can potentially alter the Si-isotope composition of diatom opal in diatamaceous sediments and sea surface Si(OH) 4. This work highlights the need for further in vitro studies into intracellular mechanisms involved in Si(OH) 4 uptake, and the associated pathways for Si-isotope fractionation in diatoms.
“…Model 2 is a second-order equation (2) that considers two pools of organic matter with different reactivities. It is similar to the equation that was used by Westrich and Berner (1984) for carbon degradation, and more recently it has also been employed for bSiO 2 dissolution (Moriceau et al, 2009;Boutorh et al, 2016):…”
Section: Statistical Analysis and Estimation Of Kinetic Parametersmentioning
confidence: 99%
“…It is generally admitted that a decrease in the growth rate due to nutrient stress other than Si-limitation leads to an increase of the cellular bSiO 2 content (Martin-Jézéquel et al 2000, Claquin et al 2002. However, low Si quotas have sometimes been measured for nutrientstressed diatoms in in situ or laboratory studies, which may partially be explained by the simultaneous decrease of the T. weissflogii cellular volume (Bucciarelli et al 2010;Lasbleiz et al 2014;Suroy et al, 2015;Boutorh et al, 2016). These results are contrary to what has been measured for T. pseudonana (Claquin et al, 2002) but agree well with what has been observed for T. weissflogii (De La Rocha et al, 2010), emphasizing the idea that diatoms of the same genus may have a different physiological response to environmental stress.…”
Section: Impact Of P-stress On the Initial Biochemical Composition Ofmentioning
Diatoms in general, and Thalassiosira weissflogii (T. weissflogii) in particular, are among the most ubiquitous phytoplanktonic species while, phosphorus (P) is an essential nutrient that limits productivity in many oceanic regimes. To investigate how T. weissflogii cultures grown under different P regimes are chemically altered before and during their prokaryotic degradation, T. weissflogii cells were cultivated under two contrasting P conditions, "P-stress" and "P-replete". Biodegradation experiments were conducted in natural seawater comprising a natural prokaryotic community. The particulate fraction was monitored for 3 weeks for organic carbon (POC), nitrogen (PON), biogenic silica (bSiO 2), total carbohydrates (PCHO) and individual monosaccharides, including prokaryotic counting. Our results indicated that P-stress induced changes in the chemical composition of the T. weissflogii cells, causing a decrease to the Si/N (1.1 to 0.46) and Si/C (0.17 to 0.08) ratios. The "P-stress T. weissflogii" cells were characterized by high amounts of galactose (23% of PCHO), xylose (21%), and glucose (19%) compared to the "P-replete T. weissflogii" cells, which were dominated by ribose (20% of PCHO), further indicating the exhaustion of riboserich molecules (e.g., ATP) in T. weissflogii under "P-stress" conditions. The degradation experiments showed that bSiO 2 produced under "P-stress" conditions dissolved more rapidly than bSiO 2 formed under "P-replete" conditions, whereas POC and PON exhibited higher degradation rate constants in the "P-replete T. weissflogii" than in the "P-stress T. weissflogii" experiment. Overall, these observations show that T. weissflogii submitted to P-limitation, results in changes in its initial biochemical composition, increases frustule dissolution rate, and decreases the degradation of T. weissflogii-organic matter by marine prokaryotes.
“…All batches were incubated in the dark, at 16 • C, during 30 days on a shaking table for continuous agitation, allowing for a better homogenization of the particles in the batch. Batch cultures were kept ajar during the 30 days, in order to preserve gases exchanges, which have been proven to limit CO 2 surplus and pH changes (Suroy et al, 2014(Suroy et al, , 2015Boutorh et al, 2016). The dSi concentrations were measured on a daily basis for 4 days, and every second day until the end of the experiment.…”
Section: Dissolution Experimentsmentioning
confidence: 99%
“…Diatom frustules are surrounded by an organic coating that needs to be removed by prokaryotes before dissolution of the frustule can begin (Bidle and Azam, 2001). In addition, biogenic silica dissolution depends on nutritive growth conditions of the diatoms (Boutorh et al, 2016). The process of silicification is known to be influenced by stressful conditions, such as nutrient limitation (Boyle, 1998;Takeda, 1998;Lasbleiz et al, 2014) and/or the presence of grazers (Pondaven et al, 2007).…”
Diatom production is mainly supported by the dissolution of biogenic silica (bSiO 2) within the first 200 m of the water column. The upper oceanic layer is enriched in dissolved and/or colloidal organic matter, such as exopolymeric polysaccharides (EPS) and transparent exopolymeric particles (TEP) excreted by phytoplankton in large amounts, especially at the end of a bloom. In this study we explored for the first time the direct influence of TEP-enriched diatom excretions on bSiO 2 dissolution. Twelve dissolution experiments on fresh and fossil diatom frustules were carried out on seawater containing different concentrations of TEP extracted from diatom cultures. Fresh diatom frustules were cleaned from the organic matter by low ash temperature, and fossil diatoms were made from diatomite powder. Results confirm that newly formed bSiO 2 dissolved at a faster rate than fossil diatoms due to a lower aluminum (Al) content. Diatom excretions have no effect on the dissolution of the newly formed bSiO 2 from Chaetoceros muelleri. Reversely, the diatomite specific dissolution rate constant and solubility of the bSiO 2 were positively correlated to TEP concentrations, suggesting that diatom excretion may provide an alternative source of dSi when limitations arise.
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